Canonical Allele Identifier: CA136833231
Gene: LINC02571 HGNC NCBI

Linked Data

dbSNP Id: rs560295345
gnomAD v2: 6-31274170-C-T
gnomAD v3: 6-31306393-C-T
gnomAD v4: 6-31306393-C-T
MyVariant Identifiers: chr6:g.31274170C>T (hg19) chr6:g.31306393C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31306393C>T , CM000668.2:g.31306393C>T GRCh38
NC_000006.11:g.31274170C>T , CM000668.1:g.31274170C>T GRCh37
NC_000006.10:g.31382149C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926691.1:n.949+385G>A
XR_926691.2:n.965+385G>A
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